A.P. Walker

1.0k total citations · 1 hit paper
16 papers, 752 citations indexed

About

A.P. Walker is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, A.P. Walker has authored 16 papers receiving a total of 752 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 5 papers in Cellular and Molecular Neuroscience and 3 papers in Genetics. Recurrent topics in A.P. Walker's work include Muscle Physiology and Disorders (8 papers), Genetic Neurodegenerative Diseases (5 papers) and Neurogenetic and Muscular Disorders Research (3 papers). A.P. Walker is often cited by papers focused on Muscle Physiology and Disorders (8 papers), Genetic Neurodegenerative Diseases (5 papers) and Neurogenetic and Muscular Disorders Research (3 papers). A.P. Walker collaborates with scholars based in United States, United Kingdom and Canada. A.P. Walker's co-authors include Larry H. Yamaoka, Richard J. Bartlett, P. C. Gaskell, K. A. Welsh, Wu-Yen Hung, Margaret A. Pericak‐Vance, Chad Haynes, Mark J. Alberts, Seymour Grufferman and James T. Lowman and has published in prestigious journals such as Nucleic Acids Research, Neurology and Cancer.

In The Last Decade

A.P. Walker

16 papers receiving 711 citations

Hit Papers

Linkage studies in familial Alzheimer disease: evidence f... 1991 2026 2002 2014 1991 100 200 300 400 500

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
A.P. Walker United States 8 421 381 209 139 108 16 752
Rajiv Joseph United States 16 179 0.4× 316 0.8× 92 0.4× 127 0.9× 160 1.5× 36 735
J.J. Martin Belgium 18 372 0.9× 887 2.3× 134 0.6× 232 1.7× 104 1.0× 45 1.3k
H. Backhovens Belgium 15 678 1.6× 608 1.6× 178 0.9× 177 1.3× 135 1.3× 27 1.1k
Jackelien van Scheppingen Netherlands 19 233 0.6× 386 1.0× 133 0.6× 174 1.3× 138 1.3× 23 859
Adriano Jiménez‐Escrig Spain 15 177 0.4× 289 0.8× 73 0.3× 114 0.8× 86 0.8× 54 698
Susana Castro‐Blanco Spain 14 311 0.7× 262 0.7× 75 0.4× 185 1.3× 44 0.4× 16 646
Fanggeng Zou United States 13 422 1.0× 443 1.2× 282 1.3× 99 0.7× 102 0.9× 19 915
Sandra Sivilia Italy 17 262 0.6× 185 0.5× 54 0.3× 169 1.2× 42 0.4× 22 664
Sally Serneels Belgium 11 753 1.8× 402 1.1× 113 0.5× 113 0.8× 213 2.0× 14 1.0k
Travis P. Barr United States 10 252 0.6× 177 0.5× 59 0.3× 115 0.8× 27 0.3× 14 590

Countries citing papers authored by A.P. Walker

Since Specialization
Citations

This map shows the geographic impact of A.P. Walker's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by A.P. Walker with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A.P. Walker more than expected).

Fields of papers citing papers by A.P. Walker

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A.P. Walker. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by A.P. Walker. The network helps show where A.P. Walker may publish in the future.

Co-authorship network of co-authors of A.P. Walker

This figure shows the co-authorship network connecting the top 25 collaborators of A.P. Walker. A scholar is included among the top collaborators of A.P. Walker based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with A.P. Walker. A.P. Walker is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

16 of 16 papers shown
1.
Walker, A.P., Nigel G. Laing, Tomoya Yamada, et al.. (1992). A TaqI map of the dystrophin gene useful for deletion and carrier status analysis.. Journal of Medical Genetics. 29(1). 14–19. 2 indexed citations
2.
Secore, Susan, A.P. Walker, Michael H. Herbstreith, et al.. (1991). A Stul polymorphism on chromosome 3p14.1 -14.2 (D3S622) defined by two polymorphic Stul sites 2.4 kb apart. Nucleic Acids Research. 19(22). 6349–6349. 1 indexed citations
3.
Laing, Nigel G., A.P. Walker, P. Anthony Akkari, et al.. (1991). Identification of duchenne muscular dystrophy genomic probe P20 constant Taq1 fragment corresponding to the EcoRV and Msp1 polymorphisms. Prenatal Diagnosis. 11(1). 63–67. 2 indexed citations
4.
Pericak‐Vance, Margaret A., P. C. Gaskell, Larry H. Yamaoka, et al.. (1991). Linkage studies in familial Alzheimer disease: evidence for chromosome 19 linkage.. PubMed. 48(6). 1034–50. 597 indexed citations breakdown →
6.
Walker, A.P., FS Collins, Teepu Siddique, et al.. (1990). D21S194, a jump clone from D21S16. Nucleic Acids Research. 18(7). 1931–1931. 5 indexed citations
7.
Yamaoka, Larry H., M. A. Pericak‐Vance, Marcy C. Speer, et al.. (1990). Tight linkage of creatine kinase (CKMM) to myotonic dystrophy on chromosome 19. Neurology. 40(2). 222–222. 15 indexed citations
8.
Ciccone, Carla, et al.. (1989). A polymorphic DNA sequence (174-3.7) on chromosome 19 [D19S58]. Nucleic Acids Research. 17(23). 10144–10144. 1 indexed citations
9.
Walker, A.P., Richard J. Bartlett, Nigel G. Laing, et al.. (1988). RFLP for Duchenne muscular dystrophy cDNA clone 30-2. Nucleic Acids Research. 16(18). 9072–9072. 3 indexed citations
10.
Laing, Nigel G., et al.. (1988). RFLP for Duchenne muscular dystrophy cDNA clone 44-1. Nucleic Acids Research. 16(14). 7209–7209. 8 indexed citations
11.
Walker, A.P. & H. S. Bachelard. (1988). Studies on DNA Damage and Repair in the Mammalian Brain. Journal of Neurochemistry. 51(5). 1394–1399. 14 indexed citations
12.
Walker, A.P., et al.. (1988). The Parental Origin of Mutations Causing Duchenne Muscular Dystrophy. Archives of Neurology. 45(1). 85–87. 5 indexed citations
13.
Hodgson, Shirley, A.P. Walker, K Hart, et al.. (1987). The application of linkage analysis to genetic counselling in families with Duchenne or Becker muscular dystrophy.. Journal of Medical Genetics. 24(3). 152–159. 17 indexed citations
14.
Hodgson, SV, A.P. Walker, Martin Bobrow, et al.. (1986). Linkage analysis using nine dna polymorphisms along the length of the x chromosome locates the gene for emery dreifuss muscular dystrophy to distal xq. Journal of Medical Genetics. 23(2). 169–170. 3 indexed citations
15.
Walker, A.P., K Hart, Charlotte G. Cole, et al.. (1986). Linkage studies in Duchenne and Becker muscular dystrophies.. Journal of Medical Genetics. 23(6). 538–547. 14 indexed citations
16.
Hart, K, Charlotte G. Cole, A.P. Walker, et al.. (1986). The screening of Duchenne muscular dystrophy patients for submicroscopic deletions.. Journal of Medical Genetics. 23(6). 516–520. 19 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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